Tag Archives: Ruben Perez

Generating clean fuel with individual gold atoms

A July 22, 2016 news item on Nanowerk highlights an international collaboration focused on producing clean fuel,

A combined experimental and theoretical study comprising researchers from the Chemistry Department and LCN [London Centre for Nanotechnology], along with groups in Argentina, China, Spain and Germany, has shed new light on the behaviour of individual gold atoms supported on defective thin cerium dioxide films – an important system for catalysis and the generation of clean hydrogen for fuel.

A July ??, 2016 LCN press release, which originated the news item, expands on the theme of catalysts, the research into individual gold atoms, and how all this could result in clean fuel,

Catalysis plays a vital role in our world; an estimated 80% of all chemical and materials are made via processes which involve catalysts, which are commonly a mixture of metals and oxides. The standard motif for these heterogeneous catalysts (where the catalysts are solid and the reactants are in the gas phase) is of a high surface area oxide support that is decorated with metal nanoparticles a few nanometres in diameter. Cerium dioxide (ceria, CeO2) is a widely used support material for many important industrial processes; metal nanoparticles supported on ceria have displayed high activities for applications including car catalytic converters, alcohol synthesis, and for hydrogen production. There are two key attributes of ceria which make it an excellent active support material: its oxygen storage and release ability, and its ability to stabilise small metal particles under reaction conditions. A recent system that has been the focus of much interest has been that of gold nanoparticles and single atoms with ceria, which has demonstrated high activity towards the water-gas-shift reaction, (CO + H2O —> CO2 + H2) a key stage in the generation of clean hydrogen for use in fuel cells.

The nature of the active sites of these catalysts and the role that defects play are still relatively poorly understood; in order to study them in a systematic fashion, the researchers prepared model systems which can be characterised on the atomic scale with a scanning tunnelling microscope.

Figure: STM images of CeO2-x(111) ultrathin films before and after the deposition of Au single atoms at 300 K. The bright lattice is from the oxygen atoms at the surface – vacancies appear as dark spots

These model systems comprised well-ordered, epitaxial ceria films less than 2 nm thick, prepared on a metal single crystal, upon which single atoms and small clusters of gold were evaporated onto under ultra-high-vacuum (essential to prevent contamination of the surfaces). Oxygen vacancy defects – missing oxygen atoms in the top layer of the ceria – are relatively common at the surface and appear as dark spots in the STM images. By mapping the surface before and after the deposition of gold, it is possible to analyse the binding of the metal atoms, in particular there does not appear to be any preference for binding in the vacancy sites at 300 K.

Publishing their results in Physical Review Letters, the researchers combined these experimental results with theoretical studies of the binding energies and diffusion rates across the surface. They showed that kinetic effects governed the behaviour of the gold atoms, prohibiting the expected occupation of the thermodynamically more stable oxygen vacancy sites. They also identified electron transfer between the gold atoms and the ceria, leading to a better understanding of the diffusion phenomena that occur at this scale, and demonstrated that the effect of individual surface defects may be more minor than is normally imagined.

Here’s a link to and a citation for the paper,

Diffusion Barriers Block Defect Occupation on Reduced CeO2(111) by P.G. Lustemberg, Y. Pan, B.-J. Shaw, D. Grinter, Chi Pang, G. Thornton, Rubén Pérez, M. V. Ganduglia-Pirovano, and N. Nilius. Phys. Rev. Lett. Vol. 116, Iss. 23 — 10 June 2016 2016DOI:http://dx.doi.org/10.1103/PhysRevLett.116.236101 Published 9 June 2016

This paper is behind a paywall.

Characterizing anatase titanium dixoide at the nanoscale

An international collaboration of researchers combined atomic force microscopy (AFM) and scanning tunneling microscopy (STM) to characterize anatase titanium dixoxide. From a Sept. 14, 2015 news item on Azonano,

A [Japan National Institute for Materials Science] NIMS research team successfully identified the atoms and common defects existing at the most stable surface of the anatase form of titanium dioxide by characterizing this material at the atomic scale with scanning probe microscopy. This work was published under open access policy in the online version of Nature Communications on June 29, 2015.

A June 29, 2015 NIMS press release, which originated the news item, includes the paper’s abstract in numbered point form,

  1. The research team consisting of Oscar Custance and Tomoko Shimizu, group leader and senior scientist, respectively, at the Atomic Force Probe Group, NIMS, Daisuke Fujita and Keisuke Sagisaka, group leader and senior researcher, respectively, at the Surface Characterization Group, NIMS, and scientists at Charles University in the Czech Republic, Autonomous University of Madrid in Spain, and other organizations combined simultaneous atomic force microscopy (AFM) and scanning tunneling microscopy (STM) measurements with first-principles calculations for the unambiguous identification of the atomic species at the most stable surface of the anatase form of titanium dioxide (hereinafter referred to as anatase) and its most common defects.
  2. In recent years, anatase has attracted considerable attention, because it has become a pivotal material in devices for photo-catalysis and for the conversion of solar energy to electricity. It is extremely challenging to grow large single crystals of anatase, and most of the applications of this material are in the form of nano crystals. To enhance the catalytic reactivity of anatase and the efficiency of devices for solar energy conversion based on anatase, it is critical to gain in-depth understanding and control of the reactions taking place at the surface of this material down to the atomic level. Only a few research groups worldwide possess the technology to create proper test samples and to make in-situ atomic-level observations of anatase surfaces.
  3. In this study, the research team used samples obtained from anatase natural single crystals extracted from naturally occurring anatase rocks. The team characterized the (101) surface of anatase at atomic level by means of simultaneous AFM and STM. Using single water molecules as atomic markers, the team successfully identified the atomic species of this surface; result that was additionally confirmed by the comparison of simultaneous AFM and STM measurements with the outcomes of first-principles calculations.
  4. In regular STM, in which an atomically sharp probe is scanned over the surface by keeping constant an electrical current flowing between them, it is difficult to stably image anatase surfaces as this material presents poor electrical conductivity over some of the atomic positions of the surface. However, simultaneous operation of AFM and STM allowed imaging the surface with atomic resolution even within the materials band gap (a region where the flow of current between the probe and the surface is, in principle, prohibited). Here, the detection of inter-atomic forces between the last atom of the atomically sharp probe and the atoms of the surface by AFM was of crucial importance. By regulating the probe-surface distance using AFM, it was possible to image the surface at atomic-scale while collecting STM data over both conductive and not conductive areas of the surface. By comparing simultaneous AFM and STM measurements with theoretical simulations, the team was not only able to discern which atomic species were contributing to the AFM and the STM images but also to identify the most common defects found at the surface.
  5. In the future, based on the information gained from this study, the NIMS research team will conduct research on molecules of technologically relevance that adsorb on anatase and characterize these hybrid systems by using simultaneous AFM and STM. Their ultimate goal is to formulate novel approaches for the development of photo-catalysts and solar cell materials and devices.

Here’s a link to and a citation for the paper,

Atomic species identification at the (101) anatase surface by simultaneous scanning tunnelling and atomic force microscopy by Oleksandr Stetsovych, Milica Todorović, Tomoko K. Shimizu, César Moreno, James William Ryan, Carmen Pérez León, Keisuke Sagisaka, Emilio Palomares, Vladimír Matolín, Daisuke Fujita, Ruben Perez, & Oscar Custance. Nature Communications 6, Article number: 7265 doi:10.1038/ncomms8265 Published 29 June 2015

This is an open access paper.